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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 1
2006 2
2007 2
2008 3
2009 1
2010 6
2011 3
2012 4
2013 5
2014 2
2015 1
2016 1
2017 1
2018 2
2019 2
2020 3
2021 9
2022 4
2023 0
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50 results
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Page 1
Usher Syndrome: Genetics of a Human Ciliopathy.
Fuster-García C, García-Bohórquez B, Rodríguez-Muñoz A, Aller E, Jaijo T, Millán JM, García-García G. Fuster-García C, et al. Among authors: jaijo t. Int J Mol Sci. 2021 Jun 23;22(13):6723. doi: 10.3390/ijms22136723. Int J Mol Sci. 2021. PMID: 34201633 Free PMC article. Review.
Prevalent ALMS1 Pathogenic Variants in Spanish Alström Patients.
Bea-Mascato B, Solarat C, Perea-Romero I, Jaijo T, Blanco-Kelly F, Millán JM, Ayuso C, Valverde D. Bea-Mascato B, et al. Among authors: jaijo t. Genes (Basel). 2021 Feb 16;12(2):282. doi: 10.3390/genes12020282. Genes (Basel). 2021. PMID: 33669459 Free PMC article.
Expanding the Genetic Landscape of Usher-Like Phenotypes.
Fuster-García C, García-García G, Jaijo T, Blanco-Kelly F, Tian L, Hakonarson H, Ayuso C, Aller E, Millán JM. Fuster-García C, et al. Among authors: jaijo t. Invest Ophthalmol Vis Sci. 2019 Nov 1;60(14):4701-4710. doi: 10.1167/iovs.19-27470. Invest Ophthalmol Vis Sci. 2019. PMID: 31725169
Updating the Genetic Landscape of Inherited Retinal Dystrophies.
García Bohórquez B, Aller E, Rodríguez Muñoz A, Jaijo T, García García G, Millán JM. García Bohórquez B, et al. Among authors: jaijo t. Front Cell Dev Biol. 2021 Jul 13;9:645600. doi: 10.3389/fcell.2021.645600. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34327195 Free PMC article.
[Genetic counselling in visual and auditory disorders].
Millán JM, Aller E, Jaijo T, Grau E, Beneyto M, Nájera C. Millán JM, et al. Among authors: jaijo t. Arch Soc Esp Oftalmol. 2008 Dec;83(12):689-702. doi: 10.4321/s0365-66912008001200003. Arch Soc Esp Oftalmol. 2008. PMID: 19085640 Review. Spanish.
USH2A Gene Editing Using the CRISPR System.
Fuster-García C, García-García G, González-Romero E, Jaijo T, Sequedo MD, Ayuso C, Vázquez-Manrique RP, Millán JM, Aller E. Fuster-García C, et al. Among authors: jaijo t. Mol Ther Nucleic Acids. 2017 Sep 15;8:529-541. doi: 10.1016/j.omtn.2017.08.003. Epub 2017 Aug 12. Mol Ther Nucleic Acids. 2017. PMID: 28918053 Free PMC article.
Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome.
Vázquez-Costa JF, Payá-Montes M, Martínez-Molina M, Jaijo T, Szymanski J, Mazón M, Sopena-Novales P; ENoD Consortium; Pérez-Tur J, Sevilla T. Vázquez-Costa JF, et al. Among authors: jaijo t. Front Mol Neurosci. 2021 Aug 30;14:721047. doi: 10.3389/fnmol.2021.721047. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34526879 Free PMC article.
50 results